Archidendron lucidum, also known as the shining Archidendron, is a type of tree that belongs to the legume family. It is native to Southeast Asia and is known for its glossy leaves and fragrant flowers. This tree species is valued for its timber and is also used in traditional medicine for its various medicinal properties. It is an important part of the ecosystem and is often planted for reforestation purposes. Overall, Archidendron lucidum is a versatile and valuable tree species in the legume family.

Synonyms Top

Scientific name	Authority	First published in
Abarema lucida	(Benth.) Kosterm.	Bull. Organ. Natuurw. Onderz. Indonesië20: 38 (1954)
Pithecellobium lucidum	Benth.	London J. Bot.3: 207 (1844)
Albizia championii	Benth.	Hooker's J. Bot. Kew Gard. Misc.4: 79 (1852)
Feuilleea championii	(Benth.) Kuntze	Revis. Gen. Pl.1: 185 (1891)

Common names Top

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Language	Common/alternative name
Chinese	亮叶猴耳环
Chinese	亮葉猴耳環
Chinese	尿桶弓
Chinese	頷垂豆
Chinese	颔垂豆
Chinese	一种维管植物

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indo-China
  - Cambodia
  - Laos
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000192038
Tropicos	13066463
KEW	urn:lsid:ipni.org:names:475074-1
The Plant List	ild-38602
Open Tree Of Life	847633
NCBI Taxonomy	1009333
IUCN Red List	147617274
IPNI	475074-1
iNaturalist	427929
GBIF	2941456
Freebase	/m/0kbhd75
EOL	646661
USDA GRIN	460574
Wikipedia	Archidendron_lucidum
CMAUP	NPO4000

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

Damage by typhoon Hato compared among three different plant communities in Macau, China

Yi Q, Ye W, Wang F, Xing F, Harris A, Duan L, Chen H

Ecol Evol

05-Oct-2023

PMCID:	PMC10555504
doi:	10.1002/ece3.10574
PMID:	37809357

Implementation of machine learning in DNA barcoding for determining the plant family taxonomy

Riza LS, Zain MI, Izzuddin A, Prasetyo Y, Hidayat T, Abu Samah KA

Heliyon

21-Sep-2023

PMCID:	PMC10520734
doi:	10.1016/j.heliyon.2023.e20161
PMID:	37767518

Shift of Host Range for the Immature Stages of the Lanternfly, Pyrops watanabei (Matsumura) (Hemiptera, Fulgoridae) Native to Taiwan

Hsu MH, Yang YL, Wu ML, Wang LJ

Insects

12-Sep-2022

PMCID:	PMC9500622
doi:	10.3390/insects13090826
PMID:	36135527

Pest categorisation of Diaphorina citri

Bragard C, Dehnen‐Schmutz K, Di Serio F, Gonthier P, Jacques M, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Kertesz V, Streissl F, MacLeod A

EFSA J

06-Jan-2021

PMCID:	PMC7786542
doi:	10.2903/j.efsa.2021.6357
PMID:	33437319

Anti-Inflammatory Activity of Extracts and Pure Compounds Derived from Plants via Modulation of Signaling Pathways, Especially PI3K/AKT in Macrophages

Merecz-Sadowska A, Sitarek P, Śliwiński T, Zajdel R

Int J Mol Sci

16-Dec-2020

PMCID:	PMC7766727
doi:	10.3390/ijms21249605
PMID:	33339446

Hybrid capture of 964 nuclear genes resolves evolutionary relationships in the mimosoid legumes and reveals the polytomous origins of a large pantropical radiation

Koenen EJ, Kidner C, de Souza ÉR, Simon MF, Iganci JR, Nicholls JA, Brown GK, de Queiroz LP, Luckow M, Lewis GP, Pennington RT, Hughes CE

Am J Bot

30-Nov-2020

PMCID:	PMC7839790
doi:	10.1002/ajb2.1568
PMID:	33253423

Cytotoxic triterpenoid saponins acylated with monoterpenic acid from Pithecellobium lucidum.

Ma SG, Hu YC, Yu SS, Zhang Y, Chen XG, Liu J, Liu YX

J Nat Prod

01-Jan-2008

doi:	10.1021/NP0703794
PMID:	18095653

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-6-[[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-[(2E,6S)-6-hydroxy-2-(hydroxymethyl)-6-methylocta-2,7-dienoyl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163038774	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(C)(C=C)O)CO)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O)O	1713.80	unknown	https://doi.org/10.1021/NP0703794
[(2S,3R,4S,5R,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5R,6R)-6-[[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-3-[(2E,6S)-2-(hydroxymethyl)-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyocta-2,7-dienoyl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163105195	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(O3)CO)O)O)C)OC4C(C(C(OC4OC(=O)C56CCC7(C(=CCC8C7(CCC9C8(CCC(C9(C)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)C)O)O)OC1C(C(C(CO1)O)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)C)C5CC(C(C6)OC(=O)C(=CCCC(C)(C=C)OC1C(C(C(C(O1)C)O)O)O)CO)(C)C)C)CO)O)O)O)O)O)O	1990.10	unknown	https://doi.org/10.1021/NP0703794
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[(1R,2R,3S,4R,5R)-2,3,4-trihydroxy-5-(hydroxymethyl)cyclohexyl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (3R,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-[[(2R,3R,4S,5R,6S)-4,5,6-trihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-hydroxy-3-[(2E,6S)-2-(hydroxymethyl)-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyocta-2,7-dienoyl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163106599	Click to see CC1C(C(C(C(O1)OC(C)(CCC=C(CO)C(=O)OC2CC3(C(CC2(C)C)C4=CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(C(O7)COC8C(C(C(C(O8)O)O)O)OC9C(C(C(CO9)O)O)O)O)O)NC(=O)C)C)C(=O)OC1C(C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)C)OC1C(C(C(O1)CO)O)O)OC1CC(C(C(C1O)O)O)CO)O)C=C)O)O)O	1901.00	unknown	https://doi.org/10.1021/NP0703794
[(2S,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6S)-5-[(2S,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3-hydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl] (3S,4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-4,5-dihydroxy-6-methyl-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-3-[(2E,6S)-2-(hydroxymethyl)-6-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyocta-2,7-dienoyl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162804549	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(O3)CO)O)O)C)OC4C(C(C(OC4OC(=O)C56CC(C(CC5C7=CCC8C9(CCC(C(C9CCC8(C7(CC6O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)C)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC(=O)C(=CCCC(C)(C=C)OC1C(C(C(C(O1)C)O)O)O)CO)CO)O)O)O)O)O)O	1844.00	unknown	https://doi.org/10.1021/NP0703794
Pithelucoside A	44448255	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(O3)CO)O)O)C)OC4C(C(C(OC4OC(=O)C56CC(C(CC5C7=CCC8C9(CCC(C(C9CCC8(C7(CC6O)C)C)(C)C)OC1C(C(C(C(O1)COC1C(C(C(C(O1)C)O)O)OC1C(C(C(CO1)O)O)O)O)O)O)C)(C)C)OC(=O)C(=CCCC(C)(C=C)OC1C(C(C(C(O1)C)O)O)O)CO)CO)O)O)O)O)O)O	1844.00	unknown	https://doi.org/10.1021/NP0703794
Pithelucoside C	24770289	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CC(C7(C6CC(C(C7)OC(=O)C(=CCCC(=CCO)C)CO)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)C)OC1C(C(C(O1)CO)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)C)O)O)O)OC1C(C(C(CO1)O)O)O)O)O	1713.80	unknown	https://doi.org/10.1021/NP0703794
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
{[2-Hydroxy-1,1-bis(hydroxymethyl)ethyl]ammonio}acetate	6992779	Click to see C(C(=O)[O-])[NH2+]C(CO)(CO)CO	179.17	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B	5316860	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO	372.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine	190	Click to see C1=NC2=NC=NC(=C2N1)N	135.13	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
1-(3-(6,7-Dimethoxyisoquinolin-1-yl)propyl)guanidine	10062645	Click to see COC1=C(C=C2C(=C1)C=CN=C2CCCN=C(N)N)OC	288.34	unknown	via CMAUP database
2-[3-[4-[4-(Diaminomethylideneamino)butyl]-6,7-dimethoxyisoquinolin-1-yl]propyl]guanidine	10069639	Click to see COC1=C(C=C2C(=C1)C(=CN=C2CCCN=C(N)N)CCCCN=C(N)N)OC	401.50	unknown	via CMAUP database
8,9-dimethoxy-2,3-dihydro-1H-pyrrolo[2,1-a]isoquinolin-4-ium	10105261	Click to see COC1=C(C=C2C3=[N+](CCC3)C=CC2=C1)OC	230.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(+)-Crispine A	11673094	Click to see COC1=C(C=C2C3CCCN3CCC2=C1)OC	233.31	unknown	via CMAUP database
2-[3-[(1S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]propyl]guanidine	24823534	Click to see COC1=C(C=C2C(NCCC2=C1)CCCN=C(N)N)OC	292.38	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]chromen-4-one	21721958	Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O	432.40	unknown	via CMAUP database
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	11377340	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)CO)O)O)O)O)O	666.60	unknown	via CMAUP database
Linariifolioside	5492485	Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O	652.60	unknown	via CMAUP database

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Archidendron lucidum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top